A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611357



Internal ID21803404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49819112..49819198hg38UCSC Ensembl
chr13:50393248..50393334hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036191
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611357
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer